Frozen Oysters: 1) I.Q.F. 2 LB/12 Frozen Oyster (Permit #NJ36RS) - Item #33200115.; I.Q.F. (T-Size) 8 oz/40 Frozen Oyster (Permit #NJ36RS...
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1673-2012.
Inspectional evidence and sample analyses as well as reports of food borne illness outbreaks due to norovirus have led FDA to believe that Korean molluscan shellfish and products containing KMS as ingredients are adulterated under Section 40(a)(4) in that they were prepared and held under insanitary conditions, whereby they may have become contaminated with filth or whereby they may have been rend
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1673-2012.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Grand Supercenter Inc. or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1673-2012.
Grand Supercenter Inc.
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
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If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
Grand Supercenter Inc. Recall FAQ
Grand Supercenter Inc. is the subject of a seafood safety report: Frozen Oysters: 1) I.Q.F. 2 LB/12 Frozen Oyster (Permit #NJ36RS) - Item #33200115.; I.Q.F. (T-Size) 8 oz/40 Frozen Oyster (Permit #NJ36RS.... The notice was published on May 18, 2012 by the U.S. Food and Drug Administration (FDA). Approximately 218,470 units are potentially affected.